Linkstation MINI Evaluation Kit 05000-500-B

GUDID 00816818022635

LinkStation MINI Evaluation Kit with power cord for United States and Canada. Bluetooth only.

ORTHOSENSOR INC

Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit Arthroplasty force sensor display unit
Primary Device ID00816818022635
NIH Device Record Keyee113292-885b-423f-b033-8e6348988b92
Commercial Distribution StatusIn Commercial Distribution
Brand NameLinkstation MINI Evaluation Kit
Version Model NumberLinkstation MINI Evaluation Kit
Catalog Number05000-500-B
Company DUNS005788130
Company NameORTHOSENSOR INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816818022635 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ONNIntraoperative Orthopedic Joint Assessment Aid

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-06
Device Publish Date2021-04-28

On-Brand Devices [Linkstation MINI Evaluation Kit]

00816818020563LinkStation MINI Evaluation Kit with Continental Europe/ Korea power cord and additional label f
00816818020556LinkStation MINI Evaluation Kit with Switzerland power cord
00816818020549LinkStation MINI Evaluation Kit with Italy power cord
00816818020532LinkStation MINI Evaluation Kit with United Kingdom and Ireland power cord
00816818020525LinkStation MINI Evaluation Kit with Continental Europe power cord
00816818020518LinkStation MINI Evaluation Kit with Australia and New Zealand power cord
00816818020501LinkStation MINI Evaluation Kit with power cord for United States and Canada
00816818022635LinkStation MINI Evaluation Kit with power cord for United States and Canada. Bluetooth only.

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.